Differential expression profile of Th1/Th2-associated chemokines characterizes Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS']JS/TEN) and drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) as distinct entities

被引:19
作者
Miyagawa, Fumi [1 ]
Hasegawa, Ayako [1 ]
Imoto, Kyoko [1 ]
Ogawa, Kohei [1 ]
Kobayashi, Nobuhiko [1 ]
Ito, Kayoko [2 ]
Fujita, Hiroyuki [2 ]
Aihara, Michiko [2 ]
Watanabe, Hideaki [3 ]
Sueki, Hirohiko [3 ]
Tohyama, Mikiko [4 ]
Asada, Hideo [1 ]
机构
[1] Nara Med Univ, Sch Med, Dept Dermatol, Kashihara, Nara 6348522, Japan
[2] Yokohama City Univ, Grad Sch Med, Dept Environm Immunodermatol, Yokohama, Kanagawa 232, Japan
[3] Showa Univ, Sch Med, Dept Dermatol, Tokyo 142, Japan
[4] Ehime Univ, Grad Sch Med, Dept Dermatol, Matsuyama, Ehime, Japan
基金
日本学术振兴会;
关键词
ERYTHEMA MULTIFORME; DRESS-SYNDROME; TARC/CCL17; RECEPTORS; CYTOKINES; THYMUS;
D O I
10.1684/ejd.2014.2477
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) and Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) are two of a triad of severe cutaneous adverse reactions (SCAR) to drugs [1, 2]. The rapid recognition of DIHS/DRESS and SJS/TEN is essential because they are potentially life-threatening syndromes. Thus, diagnostic markers or predictive factors need to be defined. We previously reported that thymus and activationregulated chemokine (TARC/CCL17) serum levels were markedly higher in the acute stage of DIHS/DRESS than in other forms of drug eruption [3, 4]. We also demonstrated that TARC levels in the acute stage of DIHS/DRESS correlated with disease activity [3]. In this study, we attempted to identify chemokine patterns that would allow us to distinguish between the different forms of drug eruptionsand gain insight into the pathomechanisms involved.
引用
收藏
页码:87 / 89
页数:4
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